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Contralateral hyperalgesia and allodynia following intradermal capsaicin injection in man

Objectives. Contralateral responses to unilateral stimuli have been well described in animal models. These range from central sensitization to peripheral inflammatory responses. Our aim was to test for contralateral responses following unilateral intradermal capsaicin injection in man. Methods. Thre...

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Autores principales: Shenker, N. G., Haigh, R. C., Mapp, P. I., Harris, N., Blake, D. R.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518944/
https://www.ncbi.nlm.nih.gov/pubmed/18632788
http://dx.doi.org/10.1093/rheumatology/ken251
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author Shenker, N. G.
Haigh, R. C.
Mapp, P. I.
Harris, N.
Blake, D. R.
author_facet Shenker, N. G.
Haigh, R. C.
Mapp, P. I.
Harris, N.
Blake, D. R.
author_sort Shenker, N. G.
collection PubMed
description Objectives. Contralateral responses to unilateral stimuli have been well described in animal models. These range from central sensitization to peripheral inflammatory responses. Our aim was to test for contralateral responses following unilateral intradermal capsaicin injection in man. Methods. Three groups were investigated. A healthy volunteer group (1) was injected with capsaicin into the volar aspect of one forearm. A group of patients with RA (2) was also injected with capsaicin. A control group of healthy volunteers (3) was not injected with capsaicin. All groups were tested for hyperalgesia and allodynia every 10 min for 1 h following the injection using quantitative sensory testing. Results. A total of 9/14 healthy volunteers (Group 1) and 10/14 patients with RA (Group 2) demonstrated contralateral sensitization that subsided within 1 h following intradermal capsaicin injection. A total of 2/23 control subjects (Group 3) demonstrated positive responses with the monofilaments. The frequency of the contralateral responses in the experimental groups compared with the control group is significant (P < 0.05). The peak hyperalgesia was relatively delayed contralaterally compared with the ipsilateral side (35 min vs 15 min). The area of sensitization, where present, was reduced compared with the ipsilateral side (5–50%). Conclusions. This is the first demonstration of a contralateral response following a unilateral stimulus in man. Bilateral neural pathways mediating contralateral responses may have a role in the pathophysiology of chronically painful or inflammatory diseases and a confounding influence on using the contralateral limb as a control experimentally. We did not find that a systemic inflammatory disease sensitized for this phenomenon.
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spelling pubmed-25189442009-02-25 Contralateral hyperalgesia and allodynia following intradermal capsaicin injection in man Shenker, N. G. Haigh, R. C. Mapp, P. I. Harris, N. Blake, D. R. Rheumatology (Oxford) Clinical Objectives. Contralateral responses to unilateral stimuli have been well described in animal models. These range from central sensitization to peripheral inflammatory responses. Our aim was to test for contralateral responses following unilateral intradermal capsaicin injection in man. Methods. Three groups were investigated. A healthy volunteer group (1) was injected with capsaicin into the volar aspect of one forearm. A group of patients with RA (2) was also injected with capsaicin. A control group of healthy volunteers (3) was not injected with capsaicin. All groups were tested for hyperalgesia and allodynia every 10 min for 1 h following the injection using quantitative sensory testing. Results. A total of 9/14 healthy volunteers (Group 1) and 10/14 patients with RA (Group 2) demonstrated contralateral sensitization that subsided within 1 h following intradermal capsaicin injection. A total of 2/23 control subjects (Group 3) demonstrated positive responses with the monofilaments. The frequency of the contralateral responses in the experimental groups compared with the control group is significant (P < 0.05). The peak hyperalgesia was relatively delayed contralaterally compared with the ipsilateral side (35 min vs 15 min). The area of sensitization, where present, was reduced compared with the ipsilateral side (5–50%). Conclusions. This is the first demonstration of a contralateral response following a unilateral stimulus in man. Bilateral neural pathways mediating contralateral responses may have a role in the pathophysiology of chronically painful or inflammatory diseases and a confounding influence on using the contralateral limb as a control experimentally. We did not find that a systemic inflammatory disease sensitized for this phenomenon. Oxford University Press 2008-09 2008-07-16 /pmc/articles/PMC2518944/ /pubmed/18632788 http://dx.doi.org/10.1093/rheumatology/ken251 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical
Shenker, N. G.
Haigh, R. C.
Mapp, P. I.
Harris, N.
Blake, D. R.
Contralateral hyperalgesia and allodynia following intradermal capsaicin injection in man
title Contralateral hyperalgesia and allodynia following intradermal capsaicin injection in man
title_full Contralateral hyperalgesia and allodynia following intradermal capsaicin injection in man
title_fullStr Contralateral hyperalgesia and allodynia following intradermal capsaicin injection in man
title_full_unstemmed Contralateral hyperalgesia and allodynia following intradermal capsaicin injection in man
title_short Contralateral hyperalgesia and allodynia following intradermal capsaicin injection in man
title_sort contralateral hyperalgesia and allodynia following intradermal capsaicin injection in man
topic Clinical
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518944/
https://www.ncbi.nlm.nih.gov/pubmed/18632788
http://dx.doi.org/10.1093/rheumatology/ken251
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